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Pharmacokinetic and Pharmacodynamic ...
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Sharma, Ankur.
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Pharmacokinetic and Pharmacodynamic Characterization of Sheta2, A Novel Orally Bioavailable Anti-Cancer Drug Towards Clinical Translation.
Record Type:
Electronic resources : Monograph/item
Title/Author:
Pharmacokinetic and Pharmacodynamic Characterization of Sheta2, A Novel Orally Bioavailable Anti-Cancer Drug Towards Clinical Translation./
Author:
Sharma, Ankur.
Published:
Ann Arbor : ProQuest Dissertations & Theses, : 2017,
Description:
190 p.
Notes:
Source: Dissertation Abstracts International, Volume: 78-09(E), Section: B.
Contained By:
Dissertation Abstracts International78-09B(E).
Subject:
Pharmaceutical sciences. -
Online resource:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10257485
ISBN:
9781369714371
Pharmacokinetic and Pharmacodynamic Characterization of Sheta2, A Novel Orally Bioavailable Anti-Cancer Drug Towards Clinical Translation.
Sharma, Ankur.
Pharmacokinetic and Pharmacodynamic Characterization of Sheta2, A Novel Orally Bioavailable Anti-Cancer Drug Towards Clinical Translation.
- Ann Arbor : ProQuest Dissertations & Theses, 2017 - 190 p.
Source: Dissertation Abstracts International, Volume: 78-09(E), Section: B.
Thesis (Ph.D.)--The University of Oklahoma Health Sciences Center, 2017.
SHetA2 is a flexible heteroarotinoid (Flex-Het), which was selected as a lead from a series of Flex-Het based on potent induction of apoptosis in cancer cells. With the promising preclinical safety and efficacy profiles, SHetA2 is now moved forward for clinical development. Well-designed experiments in preclinical animal models and utilization of physiologically, mechanism-based pharmacokinetic and pharmacodynamic (PBPK/PD) models can provide better quantitation and prediction of the disposition and dynamics of SHetA2. The main goal of this thesis was to develop PBPK/PD models for SHetA2 that not only can provide improved understanding of SHetA2 PK/PD but also can assist more rationale design of Phase 0/I clinical trials of SHetA2, thereby decreasing risk of failure at the clinical development stage and making the clinical trial cost effective. (Abstract shortened by ProQuest.).
ISBN: 9781369714371Subjects--Topical Terms:
3173021
Pharmaceutical sciences.
Pharmacokinetic and Pharmacodynamic Characterization of Sheta2, A Novel Orally Bioavailable Anti-Cancer Drug Towards Clinical Translation.
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SHetA2 is a flexible heteroarotinoid (Flex-Het), which was selected as a lead from a series of Flex-Het based on potent induction of apoptosis in cancer cells. With the promising preclinical safety and efficacy profiles, SHetA2 is now moved forward for clinical development. Well-designed experiments in preclinical animal models and utilization of physiologically, mechanism-based pharmacokinetic and pharmacodynamic (PBPK/PD) models can provide better quantitation and prediction of the disposition and dynamics of SHetA2. The main goal of this thesis was to develop PBPK/PD models for SHetA2 that not only can provide improved understanding of SHetA2 PK/PD but also can assist more rationale design of Phase 0/I clinical trials of SHetA2, thereby decreasing risk of failure at the clinical development stage and making the clinical trial cost effective. (Abstract shortened by ProQuest.).
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http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10257485
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